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Table 2 Effective allele frequency distribution and EFEMP1 variant showing association with VV in South Asian Indians

From: Replication study identified EFEMP1 association with varicose vein predisposition among Indians

CHR

SNP

BP

OR

L95

U95

p-value

CES

OR

2

rs3791679

56,096,892

1.43

1.04

1.97

0.03

2.73

(1.75–4.23)

2

rs59985551

56,106,928

1.42

1.03

1.97

0.03

2

rs3791675

56,111,309

1.42

1.03

1.96

0.03

2

rs11125610

56,117,614

1.58

1.05

2.37

0.03

p-value < 0.0001

2

rs3791665

56,126,509

0.37

0.16

0.86

0.02

2

rs1430197

56,134,827

1.36

1.00

1.83

0.05

  1. CHR chromosome, SNP single nucleotide polymorphism, BP base pairs, EA effective allele, EAF effective allele frequency, CES cumulative effect of SNPs calculated using MDR with a balanced accuracy of > 0.75 and specificity and sensitivity of > 0.80, OR Odds ratio